Literature DB >> 3758251

Cerebellar Purkinje cell activity related to the classically conditioned nictitating membrane response.

N E Berthier, J W Moore.   

Abstract

Because of the purported critical role of cerebellar lobule HVI in classical conditioning of the nictitating membrane response of the rabbit, we recorded extracellularly from HVI Purkinje cells (PCs) during differential conditioning. Rabbits were trained using tonal conditioned stimuli (CSs) and stimulation of the periocular region as the unconditioned stimulus (US). Many PCs responded to the US, the most frequently observed response being a burst of simple spikes. PCs in HVI showed a variety of responses to CSs that were related to conditioned responses (CRs). The most frequently observed response was an increase in simple spikes correlated with CRs. The activity of many of these cells antedated CRs by 20-200 ms. A smaller proportion of cells exhibited inhibition of simple spike activity that antedated CRs. The existence of PCs that alter their firing before CRs suggests that they may be causally involved in this behavior, and in this respect they reinforce reports that lesions of HVI or its connections disrupt nictitating membrane CRs. Although complex spike activity was not generally related to the US or to CRs, a few PCs responded in relation to CRs with only complex spikes. In demonstrating CR-related activity in cerebellar PCs, this study supports theories of cerebellar learning such as those of Marr and Albus.

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Year:  1986        PMID: 3758251     DOI: 10.1007/bf00236851

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  28 in total

1.  Climbing fibre inputs to cerebellar Purkinje cells from trigeminal cutaneous afferents and the SI face area of the cerebral cortex in the cat.

Authors:  T S Miles; M Wiesendanger
Journal:  J Physiol       Date:  1975-02       Impact factor: 5.182

2.  Purkinje cell activity during motor learning.

Authors:  P F Gilbert; W T Thach
Journal:  Brain Res       Date:  1977-06-10       Impact factor: 3.252

3.  Cerebellum: essential involvement in the classically conditioned eyelid response.

Authors:  D A McCormick; R F Thompson
Journal:  Science       Date:  1984-01-20       Impact factor: 47.728

4.  Long-lasting depression of parallel fiber-Purkinje cell transmission induced by conjunctive stimulation of parallel fibers and climbing fibers in the cerebellar cortex.

Authors:  M Ito; M Kano
Journal:  Neurosci Lett       Date:  1982-12-13       Impact factor: 3.046

5.  Climbing fibre induced depression of both mossy fibre responsiveness and glutamate sensitivity of cerebellar Purkinje cells.

Authors:  M Ito; M Sakurai; P Tongroach
Journal:  J Physiol       Date:  1982-03       Impact factor: 5.182

6.  Lesions of the inferior olivary complex cause extinction of the classically conditioned eyeblink response.

Authors:  D A McCormick; J E Steinmetz; R F Thompson
Journal:  Brain Res       Date:  1985-12-16       Impact factor: 3.252

7.  Somatosensory receptive fields of single units in cat cerebellar cortex.

Authors:  W T Thach
Journal:  J Neurophysiol       Date:  1967-07       Impact factor: 2.714

8.  Classical conditioning of the nictitating membrane response of the rabbit. I. Lesions of the cerebellar nuclei.

Authors:  C H Yeo; M J Hardiman; M Glickstein
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

9.  Latency of the nictitating membrane response to periocular electrostimulation in unanesthetized rabbits.

Authors:  J W Moore; J E Desmond
Journal:  Physiol Behav       Date:  1982-06

10.  Classical conditioning of the nictitating membrane response of the rabbit. IV. Lesions of the inferior olive.

Authors:  C H Yeo; M J Hardiman; M Glickstein
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

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  62 in total

1.  Developmental changes in eye-blink conditioning and neuronal activity in the cerebellar interpositus nucleus.

Authors:  J H Freeman; D A Nicholson
Journal:  J Neurosci       Date:  2000-01-15       Impact factor: 6.167

2.  Developmental changes in eye-blink conditioning and neuronal activity in the inferior olive.

Authors:  D A Nicholson; J H Freeman
Journal:  J Neurosci       Date:  2000-11-01       Impact factor: 6.167

3.  Timing mechanisms in the cerebellum: testing predictions of a large-scale computer simulation.

Authors:  J F Medina; K S Garcia; W L Nores; N M Taylor; M D Mauk
Journal:  J Neurosci       Date:  2000-07-15       Impact factor: 6.167

Review 4.  Classical eyeblink conditioning: clinical models and applications.

Authors:  J E Steinmetz; J A Tracy; J T Green
Journal:  Integr Physiol Behav Sci       Date:  2001 Jul-Sep

5.  Cerebellar cortical inhibition and classical eyeblink conditioning.

Authors:  Shaowen Bao; Lu Chen; Jeansok J Kim; Richard F Thompson
Journal:  Proc Natl Acad Sci U S A       Date:  2002-01-22       Impact factor: 11.205

Review 6.  Programs of gene expression during the laying down of memory formation as revealed by DNA microarrays.

Authors:  Sebastiano Cavallaro; Velia Dagata; Daniel L Alkon
Journal:  Neurochem Res       Date:  2002-10       Impact factor: 3.996

7.  fMRI of the conscious rabbit during unilateral classical eyeblink conditioning reveals bilateral cerebellar activation.

Authors:  Michael J Miller; Nan-kuei Chen; Limin Li; Brian Tom; Craig Weiss; John F Disterhoft; Alice M Wyrwicz
Journal:  J Neurosci       Date:  2003-12-17       Impact factor: 6.167

Review 8.  The role of interpositus nucleus in eyelid conditioned responses.

Authors:  J M Delgado-García; A Gruart
Journal:  Cerebellum       Date:  2002-12       Impact factor: 3.847

9.  Eyeblink conditioning during an interstimulus interval switch in rabbits (Oryctolagus cuniculus) using picrotoxin to disrupt cerebellar cortical input to the interpositus nucleus.

Authors:  Richard W Vogel; Jeffrey C Amundson; Derick H Lindquist; Joseph E Steinmetz
Journal:  Behav Neurosci       Date:  2009-02       Impact factor: 1.912

10.  Subcellular interactions between parallel fibre and climbing fibre signals in Purkinje cells predict sensitivity of classical conditioning to interstimulus interval.

Authors:  Jeanette Hellgren Kotaleski; David Lester; Kim T Blackwell
Journal:  Integr Physiol Behav Sci       Date:  2002 Oct-Dec
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